Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome X:134458663 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.134458663G>A

Variation displays